Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hailey S. Novis"'
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
A growing number of genes associated with Parkinson’s disease are implicated in the regulation of lysosome function, including LRRK2, whose missense mutations are perhaps the most common monogenic cause of this neurodegenerative disease. These muta
Externí odkaz:
https://doaj.org/article/f5aa1fca87a4427d8f09ae7eab0843c0
Publikováno v:
Annals of translational medicine. 10(14)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f08fe7eadab998d7a013422d34fd39d
https://pubmed.ncbi.nlm.nih.gov/35957722
https://pubmed.ncbi.nlm.nih.gov/35957722
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 14 (2020)
Frontiers in Neuroscience, Vol 14 (2020)
A growing number of genes associated with Parkinson’s disease are implicated in the regulation of lysosome function, including LRRK2, whose missense mutations are perhaps the most common monogenic cause of this neurodegenerative disease. These muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0122b063d5e6176d1b3a326da01e2c69
https://doi.org/10.3389/fnins.2020.00442
https://doi.org/10.3389/fnins.2020.00442
Autor:
Mark P. DeAndrade, Steven C. Lin, Hailey S. Novis, Anwesha Sanyal, Malú G. Tansey, Julianna J. Tomlinson, Matthew J. LaVoie, Jianjun Chang, Nathalie A. Lengacher
Publikováno v:
Mov Disord
Background Autosomal recessive mutations in the glucocerebrosidase gene, Beta-glucocerebrosidase 1 (GBA1), cause the lysosomal storage disorder Gaucher's disease. Heterozygous carriers of most GBA1 mutations have dramatically increased Parkinson's di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::942a39d45ad620a0aa13e404ca038e36
https://europepmc.org/articles/PMC8167931/
https://europepmc.org/articles/PMC8167931/
